82082-51-7 Usage
Uses
Used in Organic Synthesis:
Benzamide, 3-iodo-N-(phenylmethyl)is used as a building block in organic synthesis for creating more complex molecules. Its unique structure allows for the formation of various derivatives, making it a valuable component in the synthesis of advanced organic compounds.
Used in Pharmaceutical Development:
Benzamide, 3-iodo-N-(phenylmethyl)is used as a potential pharmaceutical candidate due to the presence of a phenylmethyl group, which has demonstrated biological activity in certain contexts. This property makes it a promising compound for the development of new drugs with therapeutic applications.
Used in Biochemical Research:
Benzamide, 3-iodo-N-(phenylmethyl)is used in biochemical research for various labeling and imaging techniques. The presence of the iodine atom in the compound makes it suitable for these applications, as it can be easily detected and tracked in biological systems. This feature is particularly useful for studying the interactions and mechanisms of complex biomolecules.
Check Digit Verification of cas no
The CAS Registry Mumber 82082-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,8 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82082-51:
(7*8)+(6*2)+(5*0)+(4*8)+(3*2)+(2*5)+(1*1)=117
117 % 10 = 7
So 82082-51-7 is a valid CAS Registry Number.
82082-51-7Relevant academic research and scientific papers
Direct amide formation from unactivated carboxylic acids and amines
Allen, C. Liana,Chhatwal, A. Rosie,Williams, Jonathan M. J.
, p. 666 - 668 (2012/01/13)
The direct coupling of unactivated carboxylic acids with amines can be performed in toluene 110 °C in the absence of catalyst. The use of simple zirconium catalysts at 5 mol% loading gave amide formation in as little as 4 h.
Potential Central Nervous System Active Agents. 1. Synthesis of Aromatic N-Benzyl Amides
Agwada, Vincent C.
, p. 479 - 481 (2007/10/02)
The preparation and spectral properties (IR, MS, NMR) are given for 18 aromatic N-benzyl amides, variously substituted on the acyl part, including four new ones and an (E)-cinnamide derivative.The amides were prepared by heating the appropriate N-benzylammonium salt in o-xylene, or from the reaction of the corresponding acid chloride with benzylamine.The occurrence of an intense peak in their mass spectra, which corresponds to the loss of the N-acyl substituent without hydrogen transfer, is reported.
